A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv153e199



Internal ID20123455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:70688979..70691578hg38UCSC Ensembl
chr10:72448735..72451334hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg382600
hg192600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2662723, esv2658231
SamplesHG00380, NA12827, HG00309, NA18870, HG01515, HG00157, NA12154, HG00152, NA12249, HG00252, NA12750, NA20787, HG00257, NA12748, NA20771, HG01250, NA20503, HG00344, NA20785, HG01519, HG01075, NA19081, NA20506, NA12342, HG01055, NA07056, HG01173, NA11920, HG00369, NA20510, NA12347, NA20544, NA20796, HG00736, NA20531, NA06989, NA20759, HG00117, HG01082, NA18953, NA20816, NA12828, HG01174, HG00139, HG00739, HG01182, NA18546, HG00106, HG01167, NA19834, NA20588, HG00111, NA18963, NA19651, HG01101, HG01168, NA19682, HG00366, NA11893, NA20798, HG00253, NA12341, NA12287, NA20521, HG00156, NA19776, HG00247, HG00256, HG00244, HG01107, NA20761, HG00158, HG00242, NA12843, HG00346, HG00250, NA20819, NA20515, NA12004, NA12383, NA19675, HG00140, HG00638, NA12155, HG00259, NA18563, NA07357, NA19900, HG01061, NA20807, NA18636, HG00141, NA12761, NA19440, NA11933, NA20541, HG00150, NA20765, HG00125, NA11831, NA12829, NA20520, HG00264, NA11995, HG00243, HG00254, NA19663, NA19679, HG00284, HG00403, NA18634, HG00237, HG00343, HG00133, NA20773, NA12751, HG00373, HG00267, HG01097, NA12046, HG00108, NA18620, NA12892, HG01516, NA20536, HG00640, NA12778, NA20826, HG00263, NA12275, HG00260, NA19664, HG00265, HG00232, HG01176, NA20818, NA11892, HG00116, HG00277, HG00103, HG01080, NA20797, NA18988, HG01070, HG00246, HG01060, HG00236, HG01149, HG00120, NA12891, NA10851, NA12890, NA20525, NA20581, HG01190, HG01334, NA20332, NA06984, HG00138, NA12889, NA19116, HG00262, HG00118, NA18971, HG00311, NA19818, NA18577, NA12878, NA18614, NA20513, NA11830, NA11992, NA19225, NA11993, NA12399, NA20812, NA12546, NA12842, NA19655, NA20543, HG01108, NA20792, HG01125, NA11829, HG01177, HG00275, NA12717, NA20528, NA19204, HG01522, HG00137, NA20806, HG00143, HG00476, NA19448, HG00271, NA20519, HG00136, NA19065, HG00126, NA07000, NA12775, HG01067, HG01198
Known GenesADAMTS14
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv153e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss204
Observed Complex0
Frequencyn/a


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